TREATMENT

Lymphangiosarcoma

LYMPHANGIOSARCOMA   ANGIOSARCOMA (LYMPHANGIOSARCOMA) Lymphangiosarcoma arises from lymph vessel endothelium. They are high grade and aggressive tumours. It usually occurs after radical lymph node dissection (Stewart – Treves syndrome) It may develop as a complication of a long standing lymphodema. CLINICAL FEATURES- Most of them occur in head and neck, breast, liver. Acute worsening of

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Lymphangiosarcoma

Lymphangiosarcoma Q. 1 Lymphangiosarcoma occurs in?  A Lymphangiomas  B Lymphomas  C Lymphedema  D Serous cavity tumors Q. 1 Lymphangiosarcoma occurs in?  A Lymphangiomas  B Lymphomas  C Lymphedema  D Serous cavity tumors Ans. C Explanation: Lymphedema REF: Sabiston 18th ed chapter 69 “Lymphangiosarcoma is a rare tumor that develops as a complication of long-standing (usually more than

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Mondor Disease

MONDOR DISEASE MONDOR’S DISEASE Mondor disease is a spontaneous thrombophlebitis of the superficial veins of the breast and anterior chest wall. Also called as String phlebitis due to tender, cord like structure. ETIOLOGY- Unknown  CLINICAL FEATURES- Presented as a thrombosed subcutaneous cord (3cm) attached to skin. On raising arm, shallow subcutaneous grooves appear alongside cord

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Mondor Disease

Mondor Disease Q. 1 Mondor’s disease of breast is a variant of:  A Mycotic infection  B Malignancy  C Thrombophlebitis  D Lymphadenitis Q. 1 Mondor’s disease of breast is a variant of:  A Mycotic infection  B Malignancy  C Thrombophlebitis  D Lymphadenitis Ans. C Explanation: Mondor’s disease is a variant of thrombophlebitis that involves the superficial veins

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